Hemophilia C is a mild form of hemophilia that does affect both sexes.
It predominantly shows up in Jewish people of the Ashkenazi decent.
It is the fourth most common coagulation disorder.
Affects 1 in 100,000 adults of the population.
What Are Some Symptoms?
Heavy nosebleeds
Frequent nosebleeds
Blood in urine
Prolonged bleeding if injured
What Kind of Mutation is Hemophilia C?
Hemophilia is a point mutation and takes places in the X chromosome. A point mutation is a type of mutation in which the replacement of a single base nucleotide with another nucleotide of the genetic material DNA or RNA.
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How Does Hemophilia Occur?
Hemophilia is an inherited bleeding disorder that prevents your blood from properly clotting.
People with hemophilia are missing the clotting factor VIII or clotting factor IX.
Hemophilia C
By: Chad DolgosTable of Contents
What is Hemophilia C?
What Are Some Symptoms?
What Kind of Mutation is Hemophilia C?
Hemophilia is a point mutation and takes places in the X chromosome. A point mutation is a type of mutation in which the replacement of a single base nucleotide with another nucleotide of the genetic material DNA or RNA.Pictures
How Does Hemophilia Occur?
Works Cited
What is Hemophilia C?What Kind of Mutation is Hemophilia C?
What Are Some Symptoms?